Allele Registry

Canonical Allele Identifier: PA658670507

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000549713

RCV001013214

RCV001107244

RCV001107245

RCV001107246

RCV001107247

RCV002491103

ClinVar Variation:

477327

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Arg600Trp	CA035694 NM_020975.6:c.1798C>T